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Trial Document Specialist (m/f)
Eingestellt von Hays aus Mannheim, Universitätsstadt
Gesuchte Skills: Support, Design
Projektbeschreibung
REFERENZNUMMER:
329552/11
IHRE AUFGABEN:
-Support Clinical Scientists in the set-up of an eTMF process for assigned studies
-Support Clinical Scientists in the maintenance of trial documentation
-Contribute to the creation/harmonization of templates/guidances, e.g. trial document delivery plan template, document tracking tools, training materials, TMF Quality Control guidances
-Assist in maintaining tracking of trial master file locations (during study and upon archiving)
IHRE QUALIFIKATIONEN:
-Good knowledge of regulatory requirements and best practices pertaining to trial document management and archiving of clinical trial documentation
-Good organizational and interpersonal skills
-Some knowledge of clinical trial design, execution and operations would be beneficial
WEITERE QUALIFIKATIONEN:
Clinical trial assistant
329552/11
IHRE AUFGABEN:
-Support Clinical Scientists in the set-up of an eTMF process for assigned studies
-Support Clinical Scientists in the maintenance of trial documentation
-Contribute to the creation/harmonization of templates/guidances, e.g. trial document delivery plan template, document tracking tools, training materials, TMF Quality Control guidances
-Assist in maintaining tracking of trial master file locations (during study and upon archiving)
IHRE QUALIFIKATIONEN:
-Good knowledge of regulatory requirements and best practices pertaining to trial document management and archiving of clinical trial documentation
-Good organizational and interpersonal skills
-Some knowledge of clinical trial design, execution and operations would be beneficial
WEITERE QUALIFIKATIONEN:
Clinical trial assistant
Projektdetails
Geforderte Qualifikationen
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Kategorie:
Medien/Design, Sonstiges